AR065931A1 - Formas cristalinas de un inhibidor de vegf-r - Google Patents

Formas cristalinas de un inhibidor de vegf-r

Info

Publication number
AR065931A1
AR065931A1 ARP080101388A ARP080101388A AR065931A1 AR 065931 A1 AR065931 A1 AR 065931A1 AR P080101388 A ARP080101388 A AR P080101388A AR P080101388 A ARP080101388 A AR P080101388A AR 065931 A1 AR065931 A1 AR 065931A1
Authority
AR
Argentina
Prior art keywords
vegf
inhibitor
crystal forms
2thite
phenylsulfanyl
Prior art date
Application number
ARP080101388A
Other languages
English (en)
Spanish (es)
Original Assignee
Pfizer Prod Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39831473&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR065931(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of AR065931A1 publication Critical patent/AR065931A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
ARP080101388A 2007-04-05 2008-04-03 Formas cristalinas de un inhibidor de vegf-r AR065931A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US91037907P 2007-04-05 2007-04-05
US97654607P 2007-10-01 2007-10-01
US3155408P 2008-02-26 2008-02-26

Publications (1)

Publication Number Publication Date
AR065931A1 true AR065931A1 (es) 2009-07-08

Family

ID=39831473

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP080101388A AR065931A1 (es) 2007-04-05 2008-04-03 Formas cristalinas de un inhibidor de vegf-r

Country Status (23)

Country Link
US (1) US8791140B2 (fr)
EP (4) EP4249063A3 (fr)
JP (2) JP5869197B2 (fr)
KR (1) KR101237588B1 (fr)
CN (2) CN101679356A (fr)
AR (1) AR065931A1 (fr)
AU (1) AU2008236444B2 (fr)
BR (1) BRPI0809471A2 (fr)
CA (1) CA2682859C (fr)
CY (1) CY1119119T1 (fr)
DK (1) DK2134702T4 (fr)
ES (2) ES2919351T3 (fr)
FI (1) FI2134702T4 (fr)
HK (1) HK1193405A1 (fr)
IL (1) IL201320A (fr)
MX (1) MX2009010761A (fr)
NZ (1) NZ580126A (fr)
PL (1) PL2134702T5 (fr)
PT (1) PT2134702T (fr)
RU (1) RU2518898C2 (fr)
SI (1) SI2134702T2 (fr)
TW (1) TWI481602B (fr)
WO (1) WO2008122858A2 (fr)

Families Citing this family (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101679356A (zh) * 2007-04-05 2010-03-24 辉瑞产品公司 适用于治疗哺乳动物异常细胞生长的6-[2-（甲基-氨甲酰基）苯基硫基]-3-e-[2-(吡啶-2-基)乙烯基]吲唑的晶型
WO2012042421A1 (fr) 2010-09-29 2012-04-05 Pfizer Inc. Procédé de traitement de la croissance cellulaire anormale
JO3062B1 (ar) * 2010-10-05 2017-03-15 Lilly Co Eli R)-(e)-2-(4-(2-(5-(1-(3، 5-داي كلورو بيريدين-4-يل)إيثوكسي)-1h-إندازول-3-يل)?ينيل)-1h-بيرازول-1-يل)إيثانول بلوري
TW201531309A (zh) * 2011-09-30 2015-08-16 Pfizer Ｎ-甲基-２-〔３-（（ｅ）-２-吡啶-２-基-乙烯基）-１ｈ-吲唑-６-基硫烷基〕苯甲醯胺之藥學組成物
WO2013068909A1 (fr) 2011-11-11 2013-05-16 Pfizer Inc. N-méthyl-2-[3-((e)-2-pyridin-2-yl-vinyl)-1h-indazol-6-ylsulfanyl]-benzamide pour le traitement de la leucémie myéloïde chronique
CA2860973C (fr) 2012-01-13 2021-10-26 Xspray Microparticles Ab Methode de production de nanoparticules hybrides amorphes stables comprenant au moins un inhibiteur de la proteine kinase et au moins un constituant polymere stabilisant et matriciel
US10098859B2 (en) 2012-09-05 2018-10-16 Amri Ssci, Llc Cocrystals of p-coumaric acid
EP2792360A1 (fr) 2013-04-18 2014-10-22 IP Gesellschaft für Management mbH (1aR,12bS)-8-cyclohexyl-11-fluoro-N-((1-methylcyclopropyl)sulfonyl)-1a-((3-methyl-3,8-diazabicyclo[3.2.1]oct-8-yl)carbonyl)-1,1a,2,2b-tetrahydrocyclopropa[d]indolo[2,1-a][2]benzazepine-5-carboxamide pour utilisation dans le traitement de HCV
CN104230886A (zh) * 2013-06-24 2014-12-24 南京华威医药科技开发有限公司 阿昔替尼新晶型
WO2015067224A1 (fr) 2013-11-08 2015-05-14 Zentiva, K.S. Sels de 6-[2- (méthylcarbamoyl) phénylsulfanyl]-3-e-[2-(pyridin-2-yl) éthanyl]indazole
CN104650034A (zh) * 2013-11-22 2015-05-27 天津市汉康医药生物技术有限公司 一种稳定的阿西替尼化合物
HUE041469T2 (hu) 2014-02-04 2019-05-28 Pfizer PD-1 antagonista és VEGFR inhibitor kombinációja rák kezelésére
JP6407257B2 (ja) * 2014-03-31 2018-10-17 千寿製薬株式会社 アルキニルインダゾール誘導体及びその用途
WO2016032927A1 (fr) 2014-08-25 2016-03-03 Pfizer Inc. Combinaison d'un antagoniste de pd-1 et d'un inhibiteur d'alk dans le traitement du cancer
SG10201810615VA (en) 2015-02-26 2019-01-30 Merck Patent Gmbh Pd-1 / pd-l1 inhibitors for the treatment of cancer
WO2016178150A1 (fr) * 2015-05-05 2016-11-10 Shilpa Medicare Limited Nouveaux polymorphes d'axitinib
CN107750166B (zh) 2015-06-16 2022-02-11 默克专利股份有限公司 Pd-l1拮抗剂组合治疗
TW201808910A (zh) * 2016-05-16 2018-03-16 帝人製藥股份有限公司 喹啉衍生物之結晶
CA3039451A1 (fr) 2016-10-06 2018-04-12 Pfizer Inc. Schema posologique d'avelumab pour le traitement du cancer
CN106883212A (zh) * 2017-03-16 2017-06-23 合肥拓锐生物科技有限公司 一种xli晶型阿昔替尼的制备方法
WO2020128893A1 (fr) 2018-12-21 2020-06-25 Pfizer Inc. Traitements combinés de cancer comprenant un agoniste de tlr
US20220226246A1 (en) 2019-05-09 2022-07-21 Synthon B.V. Pharmaceutical composition comprising axitinib
CN111187253B (zh) * 2020-01-09 2023-05-09 鲁南制药集团股份有限公司 一种阿昔替尼新晶型
WO2021195163A1 (fr) 2020-03-25 2021-09-30 Ocular Therapeutix, Inc. Implant oculaire contenant un inhibiteur de tyrosine kinase
WO2022000265A1 (fr) * 2020-06-30 2022-01-06 天津理工大学 Cocristaux d'axitinib et d'acide glutarique, et leur procédé de préparation
CN113943271B (zh) * 2020-07-15 2023-11-14 鲁南制药集团股份有限公司 一种阿昔替尼晶型及其制备方法
CN113943270B (zh) * 2020-07-15 2023-05-09 鲁南制药集团股份有限公司 一种阿昔替尼晶型
CN114685437B (zh) * 2020-12-25 2022-12-09 鲁南制药集团股份有限公司 阿昔替尼与糖精共晶
CN114685436B (zh) * 2020-12-25 2022-12-02 鲁南制药集团股份有限公司 阿昔替尼糖精共晶水合物
CN114685431B (zh) * 2020-12-26 2022-11-29 鲁南制药集团股份有限公司 一种阿昔替尼柠檬酸盐晶型
CN114685435B (zh) * 2020-12-28 2023-01-31 鲁南制药集团股份有限公司 阿昔替尼马来酸盐晶型及其制备
CN114685433B (zh) * 2020-12-28 2022-11-25 鲁南制药集团股份有限公司 一种阿昔替尼香草酸共晶盐及其制备
CN114685434B (zh) * 2020-12-28 2023-06-16 鲁南制药集团股份有限公司 一种阿昔替尼与戊二酸共晶
CN114685432B (zh) * 2020-12-28 2022-11-25 鲁南制药集团股份有限公司 阿昔替尼盐晶型及其制备方法
AU2023228391A1 (en) 2022-03-03 2024-09-19 Pfizer Inc. Multispecific antibodies binding to il-4, il-13 and/or tslp and uses thereof
EP4282415A1 (fr) 2022-05-26 2023-11-29 Genepharm S.A. Composition de comprimé stable d'axitinib

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20010306A1 (es) * 1999-07-02 2001-03-29 Agouron Pharma Compuestos de indazol y composiciones farmaceuticas que los contienen utiles para la inhibicion de proteina kinasa
US7141581B2 (en) * 1999-07-02 2006-11-28 Agouron Pharmaceuticals, Inc. Indazole compounds and pharmaceutical compositions for inhibiting protein kinases, and methods for their use
TWI262914B (en) * 1999-07-02 2006-10-01 Agouron Pharma Compounds and pharmaceutical compositions for inhibiting protein kinases
EP1248869A2 (fr) † 2000-01-07 2002-10-16 Transform Pharmaceuticals, Inc. Formation, identification et analyse a productivites elevees de formes solides diverses
US6627646B2 (en) * 2001-07-17 2003-09-30 Sepracor Inc. Norastemizole polymorphs
WO2004087152A1 (fr) 2003-04-03 2004-10-14 Pfizer Inc. Formes posologiques renfermant ag013736
WO2006048751A1 (fr) * 2004-11-02 2006-05-11 Pfizer Inc. Formes polymorphiques du 6-[2-(methylcarbamoyl)phenylsulfanyl]-3-e-[2-(pyridin-2-yl)ethenyl]indazole
RU2007116107A (ru) * 2004-11-02 2008-11-10 Пфайзер Инк. (US) Способы получения индазольных соединений
RU2007114112A (ru) 2004-11-02 2008-12-10 Пфайзер Инк. (US) Способ получения индазольных соединений
WO2006048746A2 (fr) 2004-11-02 2006-05-11 Pfizer Inc. Procedes d'evacuation de metaux lourds
CN101052633A (zh) 2004-11-02 2007-10-10 辉瑞大药厂 制备吲唑化合物的方法
CA2608952A1 (fr) 2005-05-19 2006-11-23 Dwayne Thomas Friesen Compositions pharmaceutiques comprenant une forme d'un inhibiteur vegf-r
CN101679356A (zh) 2007-04-05 2010-03-24 辉瑞产品公司 适用于治疗哺乳动物异常细胞生长的6-[2-（甲基-氨甲酰基）苯基硫基]-3-e-[2-(吡啶-2-基)乙烯基]吲唑的晶型
TW201531309A (zh) † 2011-09-30 2015-08-16 Pfizer Ｎ-甲基-２-〔３-（（ｅ）-２-吡啶-２-基-乙烯基）-１ｈ-吲唑-６-基硫烷基〕苯甲醯胺之藥學組成物

Also Published As

Publication number Publication date
CN103626739A (zh) 2014-03-12
PT2134702T (pt) 2017-07-31
TW200911781A (en) 2009-03-16
EP2134702B1 (fr) 2017-05-31
BRPI0809471A2 (pt) 2014-09-09
CA2682859C (fr) 2013-10-08
FI2134702T4 (fi) 2023-09-12
ES2634866T5 (es) 2024-03-04
RU2009136593A (ru) 2011-04-10
KR20090127949A (ko) 2009-12-14
EP3252047A3 (fr) 2018-08-15
ES2919351T3 (es) 2022-07-26
US20100179329A1 (en) 2010-07-15
MX2009010761A (es) 2009-10-28
JP2009019030A (ja) 2009-01-29
US8791140B2 (en) 2014-07-29
SI2134702T1 (sl) 2017-07-31
CN101679356A (zh) 2010-03-24
PL2134702T3 (pl) 2017-10-31
EP3252047B1 (fr) 2022-05-11
KR101237588B1 (ko) 2013-02-27
EP3252047A2 (fr) 2017-12-06
TWI481602B (zh) 2015-04-21
EP4249063A3 (fr) 2024-03-13
CY1119119T1 (el) 2018-02-14
JP2014193900A (ja) 2014-10-09
WO2008122858A9 (fr) 2009-06-18
NZ580126A (en) 2012-03-30
DK2134702T3 (en) 2017-08-21
IL201320A (en) 2016-05-31
WO2008122858A8 (fr) 2009-11-26
EP4249063A2 (fr) 2023-09-27
DK2134702T4 (da) 2023-09-25
ES2634866T3 (es) 2017-09-29
EP2134702A2 (fr) 2009-12-23
AU2008236444B2 (en) 2012-06-28
IL201320A0 (en) 2010-05-31
PL2134702T5 (pl) 2023-12-04
JP5869197B2 (ja) 2016-02-24
SI2134702T2 (sl) 2023-12-29
RU2518898C2 (ru) 2014-06-10
HK1193405A1 (zh) 2014-09-19
CN103626739B (zh) 2015-12-30
CA2682859A1 (fr) 2008-10-16
EP2134702B2 (fr) 2023-08-30
EP4074702A1 (fr) 2022-10-19
AU2008236444A1 (en) 2008-10-16
WO2008122858A3 (fr) 2009-05-07
WO2008122858A2 (fr) 2008-10-16

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